Eng B - Search Results

1

Identification of a novel beta O-thalassaemia mutation in a Greek family and subsequent prenatal diagnosis.

Waye JS, Eng B, Olivieri NF, Chui DH. Waye JS, et al. Among authors: eng b. Prenat Diagn. 1994 Oct;14(10):929-32. doi: 10.1002/pd.1970141006. Prenat Diagn. 1994. PMID: 7899267

2

Clinical course and molecular characterization of a compound heterozygote for sickle hemoglobin and hemoglobin Kenya.

Waye JS, Cai SP, Eng B, Chui DH, Francombe WH. Waye JS, et al. Among authors: eng b. Am J Hematol. 1992 Dec;41(4):289-91. doi: 10.1002/ajh.2830410413. Am J Hematol. 1992. PMID: 1283810

3

The T----C substitution at nucleotide + 1570 of the beta-globin gene is a polymorphism.

Eng B, Waye JS, Chui DH. Eng B, et al. Blood. 1992 Sep 1;80(5):1365. Blood. 1992. PMID: 1515649 Free article. No abstract available.

4

Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin gene.

Cai SP, Eng B, Francombe WH, Olivieri NF, Kendall AG, Waye JS, Chui DH. Cai SP, et al. Among authors: eng b. Blood. 1992 Mar 1;79(5):1342-6. Blood. 1992. PMID: 1536956 Free article.

5

Identification of an extensive zeta-alpha globin gene deletion in a Chinese individual.

Waye JS, Eng B, Chui DH. Waye JS, et al. Among authors: eng b. Br J Haematol. 1992 Mar;80(3):378-80. doi: 10.1111/j.1365-2141.1992.tb08148.x. Br J Haematol. 1992. PMID: 1581218

6

Human embryonic zeta-globin chain expression in deletional alpha-thalassemias.

Tang W, Luo HY, Albitar M, Patterson M, Eng B, Waye JS, Liebhaber SA, Higgs DR, Chui DH. Tang W, et al. Among authors: eng b. Blood. 1992 Jul 15;80(2):517-22. Blood. 1992. PMID: 1627804 Free article.

7

Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotype.

Waye JS, Chui DH, Eng B, Cai SP, Coleman MB, Adams JG 3rd, Steinberg MH. Waye JS, et al. Among authors: eng b. Am J Hematol. 1991 Oct;38(2):108-12. doi: 10.1002/ajh.2830380207. Am J Hematol. 1991. PMID: 1719807

8

A rapid and simple electrophoretic method for the detection of mutations involving small insertion or deletion: application to beta-thalassemia.

Cai SP, Eng B, Kan YW, Chui DH. Cai SP, et al. Among authors: eng b. Hum Genet. 1991 Oct;87(6):728-30. doi: 10.1007/BF00201734. Hum Genet. 1991. PMID: 1937477

9

High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene region.

Waye JS, Cai SP, Eng B, Clark C, Adams JG 3rd, Chui DH, Steinberg MH. Waye JS, et al. Among authors: eng b. Blood. 1991 Mar 1;77(5):1100-3. Blood. 1991. PMID: 1995096 Free article.

10

Hb FM-Fort Ripley: confirmation of autosomal dominant inheritance and diagnosis by PCR and direct nucleotide sequencing.

Hain RD, Chitayat D, Cooper R, Bandler E, Eng B, Chui DH, Waye JS, Freedman MH. Hain RD, et al. Among authors: eng b. Hum Mutat. 1994;3(3):239-42. doi: 10.1002/humu.1380030310. Hum Mutat. 1994. PMID: 7517266

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